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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs780445863

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr10:72007465 (GRCh38.p14) Help

The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.

Alleles
C>T
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.000004 (1/235724, GnomAD_exome)
T=0.000010 (1/104968, ExAC)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
CHST3 : Missense Variant
Publications
0 citations
Genomic View
See rs on genome
Help

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download
Study Population Group Sample Size Ref Allele Alt Allele
gnomAD - Exomes Global Study-wide 235724 C=0.999996 T=0.000004
gnomAD - Exomes European Sub 122292 C=0.999992 T=0.000008
gnomAD - Exomes Asian Sub 48424 C=1.00000 T=0.00000
gnomAD - Exomes American Sub 34250 C=1.00000 T=0.00000
gnomAD - Exomes African Sub 15078 C=1.00000 T=0.00000
gnomAD - Exomes Ashkenazi Jewish Sub 9784 C=1.0000 T=0.0000
gnomAD - Exomes Other Sub 5896 C=1.0000 T=0.0000
ExAC Global Study-wide 104968 C=0.999990 T=0.000010
ExAC Europe Sub 62510 C=0.99998 T=0.00002
ExAC Asian Sub 23352 C=1.00000 T=0.00000
ExAC American Sub 10414 C=1.00000 T=0.00000
ExAC African Sub 7954 C=1.0000 T=0.0000
ExAC Other Sub 738 C=1.000 T=0.000
Help

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements
Sequence name Change
GRCh38.p14 chr 10 NC_000010.11:g.72007465C>T
GRCh37.p13 chr 10 NC_000010.10:g.73767223C>T
CHST3 RefSeqGene NG_012635.1:g.48104C>T
Gene: CHST3, carbohydrate sulfotransferase 3 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
CHST3 transcript NM_004273.5:c.434C>T S [TCC] > F [TTC] Coding Sequence Variant
carbohydrate sulfotransferase 3 NP_004264.2:p.Ser145Phe S (Ser) > F (Phe) Missense Variant
CHST3 transcript variant X1 XM_006718075.5:c.434C>T S [TCC] > F [TTC] Coding Sequence Variant
carbohydrate sulfotransferase 3 isoform X1 XP_006718138.1:p.Ser145Phe S (Ser) > F (Phe) Missense Variant
CHST3 transcript variant X2 XM_011540369.3:c.434C>T S [TCC] > F [TTC] Coding Sequence Variant
carbohydrate sulfotransferase 3 isoform X1 XP_011538671.1:p.Ser145Phe S (Ser) > F (Phe) Missense Variant
CHST3 transcript variant X3 XM_047426022.1:c.434C>T S [TCC] > F [TTC] Coding Sequence Variant
carbohydrate sulfotransferase 3 isoform X1 XP_047281978.1:p.Ser145Phe S (Ser) > F (Phe) Missense Variant
Help

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar
Help

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement C= T
GRCh38.p14 chr 10 NC_000010.11:g.72007465= NC_000010.11:g.72007465C>T
GRCh37.p13 chr 10 NC_000010.10:g.73767223= NC_000010.10:g.73767223C>T
CHST3 RefSeqGene NG_012635.1:g.48104= NG_012635.1:g.48104C>T
CHST3 transcript NM_004273.5:c.434= NM_004273.5:c.434C>T
CHST3 transcript NM_004273.4:c.434= NM_004273.4:c.434C>T
CHST3 transcript variant X1 XM_006718075.5:c.434= XM_006718075.5:c.434C>T
CHST3 transcript variant X2 XM_006718075.4:c.434= XM_006718075.4:c.434C>T
CHST3 transcript variant X2 XM_006718075.3:c.434= XM_006718075.3:c.434C>T
CHST3 transcript variant X2 XM_006718075.2:c.434= XM_006718075.2:c.434C>T
CHST3 transcript variant X1 XM_006718075.1:c.434= XM_006718075.1:c.434C>T
CHST3 transcript variant X2 XM_011540369.3:c.434= XM_011540369.3:c.434C>T
CHST3 transcript variant X1 XM_011540369.2:c.434= XM_011540369.2:c.434C>T
CHST3 transcript variant X1 XM_011540369.1:c.434= XM_011540369.1:c.434C>T
CHST3 transcript variant X3 XM_047426022.1:c.434= XM_047426022.1:c.434C>T
carbohydrate sulfotransferase 3 NP_004264.2:p.Ser145= NP_004264.2:p.Ser145Phe
carbohydrate sulfotransferase 3 isoform X1 XP_006718138.1:p.Ser145= XP_006718138.1:p.Ser145Phe
carbohydrate sulfotransferase 3 isoform X1 XP_011538671.1:p.Ser145= XP_011538671.1:p.Ser145Phe
carbohydrate sulfotransferase 3 isoform X1 XP_047281978.1:p.Ser145= XP_047281978.1:p.Ser145Phe
Help

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

2 SubSNP, 2 Frequency submissions
No Submitter Submission ID Date (Build)
1 EVA_EXAC ss1689947751 Apr 01, 2015 (144)
2 GNOMAD ss2738318655 Nov 08, 2017 (151)
3 ExAC NC_000010.10 - 73767223 Oct 12, 2018 (152)
4 gnomAD - Exomes NC_000010.10 - 73767223 Jul 13, 2019 (153)
Help

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
172064, 7516696, ss1689947751, ss2738318655 NC_000010.10:73767222:C:T NC_000010.11:72007464:C:T (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs780445863

Help

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:
Select flank length:

Genomic regions, transcripts, and products
Top Help

NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Software version is: 2.0.1.post761+d5e8e07